Clinical Trial to Evaluate Efficacy and Safety of DP-R202 and Anplag in Patients With Artery Occlusive Disease

NCT ID: NCT02393612

Last Updated: 2016-11-01

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

PHASE3

Total Enrollment

151 participants

Study Classification

INTERVENTIONAL

Study Start Date

2012-10-31

Study Completion Date

2014-04-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Sarpogrelate hydrochloride, a selective 5-HT2A antagonist, has been widely used as an anti-platelet agent for the treatment of PAD. DP-R202 is a new Sarpogrelate hydrochloride product improved patient's convenience and disadvantage of dosage regimen of previous drug. The aim of this study was to compare the efficacy and safety of DP-R202 and Anplag® Tab in patients with PAD

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

1. Design This clinical trial is 12 weeks, multicenter, randomized, double-blind, parallel group, phase 3 study which registered patients in total 25 institutions appointed as national clinical trial institution, it was conducted by receiving IRB(institutional review board) approval from each institutions.

Target patients were aged over 20 years old male or female lower limb peripheral artery occlusion patients with fontaine stage II/III, who has lower limb pain or symptoms like leg stretching or numbing, lower limb pain degree is over 40 mm evaluated by VAS at screening, and ABI (ankle-brachial index) ≤0.9 or stenosis rate over \>50%, diagnosed with PAD and voluntarily agreed to participate in clinical study and signed study consent form. In addition, exclusion criteria were patients who received peripheral related surgery within 1 month of clinical study participation, Fontaine stage 4, NYHA class 3-4, uncontrollable hypertension patients (systolic BP ≥ 180 mmHg, diastolic BP ≥ 110 mmHg), patients with history of cerebrovascular disease(cerebral infarction, cerebral hemorrhage and etc.) within 6 months prior to clinical trial participation, patients with uncontrollable diabetes (HbA1c ≥ 9%), and patients with renal insufficiency (creatinine \> 3.0 mg/dL). Study subjects who met subjects criteria and recruited were total 151 subjects (study group: 75 subjects, comparator group: 76), and among these, 16 subjects (study group: 7 subjects, comparator group: 9 subjects) were dropouts therefore, total study subjects who completed study was 135 subjects (study group: 68 subjects, comparator group: 67 subjects). Dropout reasons were 'clinical trial plan violation' for 3 subjects (comparator group: 3 subjects), ' consent withdrawal' for 8 subjects( study group: 5 subjects, comparator group: 3 subjects), ' fail to follow up' for 1 subject (comparator group: 1 subject), 'adverse event' for 3 subjects ( study group: 1 subject, comparator group: 2 subjects), ' other reasons' for 1 subjects ( study group) and there was no dropout due to 'lack of efficacy'. Selected subjects were stratified by 1:1 ratio and randomly assigned to investigational product or comparator by Fontaine Stage II or Fontaine Stage III using block randomization method and double-blind was applied to both investigator and study subjects.
2. Administration Method Investigational product was DP-R202 (sarpogrelate hydrochloride 300 mg: DreamPharma, Inc.), and comparator was Anplag® Tab (sarpogrelate hydrochloride 100 mg: Yuhan Corp.). Administration period to subjects was 12 weeks, study group took investigational product, DP-R202 1 tab once(morning) and took placebo, Anplag® Tab 1 tab/once, 3 times/day, and comparator group took investigational product, Anplag® Tab 1 tab/once, 3 times/day and took DP-R202, placebo 1 tab once(morning).

Administration dosage of test drug was conducted as fixed dosage and dosage fluctuation based on subject's condition was not performed.
3. Efficacy and Safety Assessment Parameter Subjects visited at 4, 8, and 12 weeks including baseline visit (visit 2) at 4 weeks interval (total 4 times) and took efficacy and quality of life assessment.

Variation in lower limb pain (VAS) comparing baseline with 12 weeks point as a primary efficacy Assessment parameter, variation in lower limb pain (VAS) and coldness 5-point scale comparing baseline with 4, 8 weeks, ankle brachial pressure index (ABI), ankle systolic pressure (ASP), quality of life assessment index(SF-36), Maximum Walking Distance (MWD), Pain Free Walking Distance (PFWD), and investigator's general assessment(VAS) at 4, 8, and 12 weeks as secondary efficacy assessment parameters, efficacy was measured. Pain and coldness test was measured using pain and coldness felt by subject 24 hours prior to the visit, MWD and PFWD was measured only on subjects who was determined to be possible to measure, and asked to record daily degree of lower limb pain every day from baseline till the end of clinical trial only with subject who can record it. Also, adverse even, laboratory test, vital sign, weight measurement were conducted for efficacy assessment. Physical test and vital sign were conducted at screening visit, administration begins, 4, 8, and 12 weeks after administration and urine pregnancy test and laboratory test were conducted at screening visits and 12 weeks after administration. ECG test was conducted at screening visit, 4, 8, and 12 weeks after administration. Laboratory test criteria were hematological test, blood chemical test, blood coagulation test and urine test.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Peripheral Arterial Disease

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

TRIPLE

Participants Investigators Outcome Assessors

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

DP-R202

Patients administrate DP-R202 (Sarpogrelate 300mg) once a day for 12 weeks

Group Type EXPERIMENTAL

DP-R202

Intervention Type DRUG

Sarpogrelate HCl SR 300mg is administrated to patients with PAD for 12 weeks

Anplag tab

Intervention Type DRUG

Anplag tab 100mg is administrated to patients with PAD for 12 weeks

Anplag tab

Patients administrate Anplag tab (Sarpogrelate 100mg) 3 times a day for 12 weeks

Group Type ACTIVE_COMPARATOR

DP-R202

Intervention Type DRUG

Sarpogrelate HCl SR 300mg is administrated to patients with PAD for 12 weeks

Anplag tab

Intervention Type DRUG

Anplag tab 100mg is administrated to patients with PAD for 12 weeks

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

DP-R202

Sarpogrelate HCl SR 300mg is administrated to patients with PAD for 12 weeks

Intervention Type DRUG

Anplag tab

Anplag tab 100mg is administrated to patients with PAD for 12 weeks

Intervention Type DRUG

Other Intervention Names

Discover alternative or legacy names that may be used to describe the listed interventions across different sources.

Sarpogrelate HCl SR 300mg

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Lower limb pain degree is over 40 mm evaluated by VAS at screening
* ABI (ankle-brachial index) ≤0.9

Exclusion Criteria

* Patients with peripheral related surgery within 1 month of clinical study participation
* Fontaine stage 4, NYHA class 3-4
Minimum Eligible Age

20 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Alvogen Korea

INDUSTRY

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

DP-CTR202-III-04

Identifier Type: -

Identifier Source: org_study_id